🇺🇸 JEMPERLI in United States

FDA authorised JEMPERLI on 22 April 2021

Marketing authorisations

FDA — authorised 22 April 2021

  • Application: BLA761174
  • Marketing authorisation holder: GLAXOSMITHKLINE
  • Local brand name: JEMPERLI
  • Indication: INJECTABLE — INJECTION
  • Status: approved

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FDA — authorised 17 August 2021

  • Application: BLA761223
  • Marketing authorisation holder: GLAXOSMITHKLINE LLC
  • Local brand name: JEMPERLI
  • Indication: INJECTABLE — INJECTION
  • Status: approved

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FDA

  • Status: approved

JEMPERLI in other countries

Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.

Other Oncology approved in United States

Frequently asked questions

Is JEMPERLI approved in United States?

Yes. FDA authorised it on 22 April 2021; FDA authorised it on 17 August 2021; FDA has authorised it.

Who is the marketing authorisation holder for JEMPERLI in United States?

GLAXOSMITHKLINE holds the US marketing authorisation.